BEUDAMED
    5,148 results · 30ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    VENA TECH VENA CAVA FILTER

    FDA Adverse Event
    Malfunction ·B. BRAUN VENA-TECH·Product code DTK·May 12, 1998

    VENATECH

    FDA Adverse Event
    Death ·B. BRAUN MEDICAL INC.·Product code DTK·July 10, 2008

    ELECSYS 2010

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·May 17, 2007

    VENA TECH

    FDA Adverse Event
    Injury ·B. BRAUN MEDICAL, INC.·Product code DTK·August 19, 2004

    ANALYTICAL E MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LGD·June 3, 2007

    INTEGRA 700

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·April 4, 2007

    VENA TECH - LGM

    FDA Adverse Event
    Death ·*·Product code DTK·March 2, 2006

    VENA TECH-LGM

    FDA Adverse Event
    Death ·VENA TECH B. BRAUN MEDICAL·Product code DTK·October 1, 1997

    VENA TECH VENA CAVA FILTER

    FDA Adverse Event
    Malfunction ·B. BRAUN VENA-TECH·Product code DTK·April 30, 1998

    VENATECH - LGM 30D/U VENA CAVA FILTER SYSTEM

    FDA Adverse Event
    Injury ·B. BRAUN MEDICAL SAS·Product code DTK·July 24, 2007

    VENATECH - LGM 30D/U VENA CAVA FILTER SYSTEM

    FDA Adverse Event
    Other ·B. BRAUN MEDICAL SAS·Product code DTK·December 4, 2007

    ORTHO PROVUE

    FDA Adverse Event
    Malfunction ·MICRO TYPING SYSTEMS, INC.·Product code KSZ·November 2, 2009

    BRAUN VENA TECH LGM

    FDA Adverse Event
    Injury ·B BRAUN MEDICAL, INC.·Product code DTK·August 23, 1995

    LGM VENA CAVA FILTER

    FDA Adverse Event
    Injury ·B BRAUN VENA-TECH·Product code DTK·February 5, 1996

    SARS-COV-2 IGM

    FDA Adverse Event
    Malfunction ·ABBOTT IRELAND·Product code QKO·March 9, 2021

    VENA TECH

    FDA Adverse Event
    Injury ·B. BRAUN MEDICAL, INC.·Product code DTK·August 2, 2004

    GLOVER, EXAMINING, LG, M, & SM.

    FDA Adverse Event
    Malfunction ·SPECTRUM LABORATORIES, INC.·Product code LYY·June 20, 1997

    UNKNOWN DEPUY LG M/B PATELLA

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code NJL·January 3, 2017

    KENE LG M/B PATELLAR DOME

    FDA Adverse Event
    Injury ·HOWMEDICA, INC.·Product code HTG·February 14, 1997

    VENA TECH LGM VENA CAVA FILTER

    FDA Adverse Event
    Death ·B. BRAUM MEDICAL INC·Product code DTK·July 13, 2001